M2A MAGNUM 12/14 TAPER INSERTS AND ONE-PIECE MODULAR HEADS— 510(k) K061423

Substantially Equivalent

Biomet Manufacturing Corp

FDA 510(k) clearance K061423 for M2A MAGNUM 12/14 TAPER INSERTS AND ONE-PIECE MODULAR HEADS, Substantially Equivalent on 2006-07-27. Applicant: Biomet Manufacturing Corp.

Clearance details

Applicant: Biomet Manufacturing Corp
Product code: Code KWA
Advisory panel: Orthopedic
Date received: 2006-05-23
Decision date: 2006-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KWA

product code KWA

Death: 38
Injury: 10,439
Malfunction: 1,862
Total: 12,339

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.